![Food and Drug Administration / Pharmaceutical industry / Pharmaceuticals policy / Food law / Abbreviated New Drug Application / New drug application / Federal Food / Drug / and Cosmetic Act / Generic drug / Approved Drug Products with Therapeutic Equivalence Evaluations / Center for Drug Evaluation and Research / Drug Master File Food and Drug Administration / Pharmaceutical industry / Pharmaceuticals policy / Food law / Abbreviated New Drug Application / New drug application / Federal Food / Drug / and Cosmetic Act / Generic drug / Approved Drug Products with Therapeutic Equivalence Evaluations / Center for Drug Evaluation and Research / Drug Master File](https://www.pdfsearch.io/img/b3f35537401f9b704fbec43bba44e750.jpg) Food and Drug Administration Pharmaceutical industry Pharmaceuticals policy Food law Abbreviated New Drug Application New drug application Federal Food Drug and Cosmetic Act Generic drug Approved Drug Products with Therapeutic Equivalence Evaluations Center for Drug Evaluation and Research Drug Master File | | Updating ANDA Labeling After the Marketing Application for the Reference Listed Drug Has Been Withdrawn Guidance for IndustryAdd to Reading ListSource URL: www.fda.govDownload Document from Source Website File Size: 94,11 KBShare Document on Facebook
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